Medwatch Form 3500. Triage unit sequence # fda rec. Web (form fda 3500b) form approved:
Regulatory Submissions Product Documentation
Triage unit sequence # fda rec. Web form fda 3500 may be used to report to the agency adverse events, product problems, product use errors, and therapeutic failures. • you had a sudden or unsafe effect. When do i use this form? Medwatch form is specially designed by mastercontrol to cater medical device reporting requirements. Web form fda 3500a for each suspect device. Web online using the medwatch online reporting form; • if the suspect medical device is a single use device • you were hurt or had a bad side. Web medwatch consumer reporting form 3500.
Web (form fda 3500b) form approved: • you were hurt or had a bad side. Medwatch, food and drug administration, 5600 fishers lane, rockville, md 20852; Each form fda 3500a will be given a separate manufacturer report number. November 01, 2005 for use by health professionals and consumers for voluntary reporting of adverse. For voluntary reporting of adverse events, product problems and product use/medication. Web medwatch is the fda reporting system for adverse events (aes), and form 3500a is used for adverse event reporting. The adverse event reporting system in ofni clinical makes. Web instructions for completing the medwatch form 3500 updated: Web (form fda 3500b) form approved: Report a problem caused by a medical product.
